OMOP Concept 4103381
Retinitis pigmentosa
StandardConditionSNOMED28835009Disorder
Maps from
14
Descendants
33
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
14 source codes normalize to Retinitis pigmentosa via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 125036 | Tapetoretinal dystrophy | Non-standard |
| CIEL | 127531 | Retinitis pigmentosa | Non-standard |
| HPO | HP_0000510 | Rod-cone dystrophy | Non-standard |
| HPO | HP_0000580 | Pigmentary retinopathy | Non-standard |
| ICD10CM | H35.52 | Pigmentary retinal dystrophy | Non-standard |
| ICD9CM | 362.74 | Pigmentary retinal dystrophy | Non-standard |
| ICD9CM | 362.76 | Dystrophies primarily involving the retinal pigment epithelium | Non-standard |
| KCD7 | H35.52 | Dystrophies primarily involving the retinal pigment epithelium | Non-standard |
| MeSH | D012174 | Retinitis Pigmentosa | Non-standard |
| OXMIS | 7448RP | RETINITIS PIGMENTOSA | Non-standard |
| Read | F427600 | Retinitis pigmentosa | Non-standard |
| Read | F427L00 | Tapetoretinal dystrophy | Non-standard |
| Read | F427L11 | Tapetoretinal degeneration | Non-standard |
| UK Biobank | 6-1527 | retinitis pigmentosa | Non-standard |
Synonyms
Alternative names recorded for Retinitis pigmentosa across source vocabularies.
- retinitis pigmentaria
- retinitis pigmentaria (trastorno)
- Retinitis pigmentosa (disorder)
- RP - Retinitis pigmentosa
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(26)Roll up to these when you need a wider cohort.
- 1Hereditary retinal dystrophy
- 2Hereditary disorder of the visual system
- 2Retinal dystrophy
- 3Degeneration of retina
- 3Hereditary disorder by system
- 3Visual system disorder
- 4Degenerative disorder of eye
- 4Disorder of body system
- 4Eye / vision finding
- 4Hereditary disease
- 4Retinal disorder
- 5Anomaly of eye
- 5Clinical finding
- 5Degenerative disorder
- 5Disease
- 5Disorder of vitreous body and/or retina
- 5Genetic disease
- 5Retina finding
- 6Disorder of eye
- 6Disorder of posterior segment of eye
- 6Globe finding
- 7Disorder of eye region
- 7Disorder of sensory organ
- 7Finding of head region
- 8Disorder of head
Showing 25 of 26. Retrieve the full set via the API.
Narrower concepts
(33)Included automatically when you query with descendants.
- 1Autosomal dominant retinitis pigmentosa
- 1Autosomal recessive retinitis pigmentosa
- 1Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome
- 1HSMN IV
- 1Hypogonadotropic hypogonadism retinitis pigmentosa syndrome
- 1NARP syndrome
- 1Retinitis pigmentosa due to systemic disease
- 1Retinitis pigmentosa of left eye
- 1Retinitis pigmentosa of right eye
- 1X-linked retinitis pigmentosa
- 2Ataxia co-occurrent and due to phytanic acid storage disease
- 2Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome
- 2Autosomal recessive posterior column ataxia and retinitis pigmentosa
- 2Chromosome Xp11.3 microdeletion syndrome
- 2Cleft lip retinopathy syndrome
- 2Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
- 2Oculotrichodysplasia
- 2Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome
- 2Primary ciliary dyskinesia and retinitis pigmentosa syndrome
- 2Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
- 2Retinitis pigmentosa-deafness syndrome
- 2Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome
- 2Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome
- 2Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome
- 2Retinitis pigmentosa of bilateral eyes
Showing 25 of 33. Retrieve the full set via the API.
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